510(k) K222203 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DualXSLIM(R) T/PLIF
| Applicant | Amplify Surgical, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 18, 2022 |
| Received | Jul 25, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222203
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.